T helper cells and efficacy of Haemophilus influenzae type b conjugate vaccination

Jodie McVernon1, N Avrion Mitchison, E Richard Moxon

  • 1Immunisation Department, Health Protection Agency, Communicable Disease Surveillance Centre, London, UK. jodie.mcvernon@hpa.org.uk

Insights

Fully vaccinated children in the UK are experiencing invasive Haemophilus influenzae type b (Hib) infections. This rise may stem from the conjugate vaccine

Area of Science:

  • Immunology
  • Vaccinology
  • Infectious Diseases
  • Public Health

Background:

  • Invasive Haemophilus influenzae type b (Hib) infections are occurring in a small number of fully vaccinated children in the UK.
  • Recent years have seen a rise in Hib disease, linked to declining vaccine-induced antibody levels in early childhood.
  • Protection increasingly relies on immunological memory, necessitating interventions like catch-up vaccination campaigns.

Purpose of the Study:

  • To investigate the reasons behind the resurgence of invasive Hib infections in vaccinated UK children.
  • To explore the potential role of vaccine-induced immune responses and natural boosting in disease incidence.
  • To assess the implications for current and future conjugate vaccine strategies.

Main Methods:

  • Analysis of invasive Hib infection cases in fully vaccinated children.
  • Evaluation of vaccine-induced antibody levels and immunological memory.
  • Assessment of Hib circulation patterns and potential impact on natural boosting.

Main Results:

  • A rise in invasive Hib infections observed in fully vaccinated children.
  • Lower vaccine-induced antibody levels noted in the first five years of life.
  • Potential contribution of impaired T cell response and reduced natural boosting to increased disease incidence.

Conclusions:

  • The conjugate vaccine's limitations in inducing specific helper T cells and reduced natural boosting may contribute to rising invasive Hib disease.
  • The findings suggest that the vaccine may not fully activate all necessary immune system components.
  • This has significant implications for the scheduling and design of other conjugate vaccines, including those for meningococcal and pneumococcal diseases.

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